首页> 美国卫生研究院文献>Antimicrobial Agents and Chemotherapy >Voriconazole Concentration in Human Aqueous Humor and Plasma during Topical or Combined Topical and Systemic Administration for Fungal Keratitis
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Voriconazole Concentration in Human Aqueous Humor and Plasma during Topical or Combined Topical and Systemic Administration for Fungal Keratitis

机译:真菌性角膜炎的局部或联合局部和全身给药过程中人体水溶液和血浆中的伏立康唑浓度

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摘要

Voriconazole (VRC) is an antifungal drug that effectively treats keratitis caused by yeasts and molds when administered orally. We retrospectively evaluated clinical outcomes and plasma and aqueous humor drug concentrations in five patients with fungal keratitis and one patient with posttraumatic endophthalmitis who were treated with VRC. VRC was administered either topically (1% eye drops every hour) or orally (400 mg twice a day). Plasma and aqueous humor samples from affected eyes were taken 12 h after oral administration or 1 h after eye drop application. The drug concentration was measured by liquid chromatography with UV or mass spectrometric detection. All six patients responded well to VRC treatment. The VRC concentration ranged from 2.93 to 3.40 mg/liter in the aqueous humor and from 3.20 to 4.20 mg/liter in the plasma after combined oral and topical treatment. Topical administration alone resulted in highly variable trough VRC concentrations of 0.61 to 3.30 mg/liter in the aqueous humor. VRC concentrations were above the MIC for Candida albicans Aspergillus fumigatus and clinical improvement was seen in all four patients with C. albicans and A. fumigatus keratitis. Combined orally and topically administered VRC resulted in aqueous humor drug concentrations of ≥2.93 mg/liter, which is above the VRC MIC for most fungi. Topical VRC treatment resulted in an aqueous humor drug concentration >0.61 mg/liter, which is above the MIC for most Candida species. The results from this small series of patients suggest that both topical and combined systemic and topical VRC therapy can be effective in treating fungal keratitis. Furthermore, the data provide preliminary support for initiation of VRC treatment with a combined topical and systemic administration until the causative fungus and its MIC are identified.
机译:伏立康唑(VRC)是一种抗真菌药物,口服时可有效治疗由酵母和霉菌引起的角膜炎。我们回顾性评估了接受VRC治疗的5例真菌性角膜炎患者和1例创伤后眼内炎患者的临床结局以及血浆和房水药物浓度。局部(每小时1%滴眼液)或口服(每天两次400 mg)口服VRC。口服给药后12小时或滴眼液后1小时,取自患眼的血浆和房水样本。药物浓度通过具有UV或质谱检测的液相色谱法测量。所有六名患者对VRC治疗反应良好。口服和局部联合治疗后,房水中的VRC浓度范围为2.93至3.40 mg / L,血浆中的VRC浓度范围为3.20至4.20 mg / L。仅局部给药导致房水中VRC浓度的高度可变为0.61至3.30 mg / L。对于白色念珠菌烟曲霉,VRC浓度高于MIC,并且在所有四例白色念珠菌和烟曲霉性角膜炎患者中均观察到临床改善。口服和局部施用VRC的结合导致房水中的药物浓度≥2.93mg / L,高于大多数真菌的VRC MIC。局部VRC处理导致房水药物浓度> 0.61 mg / L,高于大多数念珠菌物种的MIC。该小系列患者的结果表明,局部以及全身和局部VRC联合治疗均可有效治疗真菌性角膜炎。此外,这些数据为通过局部和全身联合给药开始VRC治疗提供了初步支持,直到确定了病原真菌及其MIC。

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